| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72375958-72376124 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72686129-72686225 | Common:2; Rare:35; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633046-73633573 | Common:5; Rare:189 | ||||
| chr15:73684124-73684392 | Rare:71 | ||||
| chr15:73752226-73752346 | Rare:31 | ||||
| chr15:73992153-73992389 | Rare:84 | ||||
| chr15:73994581-73994771 | Common:1; Rare:38 | ||||
| chr15:74127814-74128148 | Common:1; Rare:56 | ||||
| chr15:74130073-74130417 | Rare:77 | ||||
| chr15:74174341-74174589 | Common:3; Rare:45 | ||||
| chr15:74433828-74434079 | Common:4; Rare:81 | ||||
| chr15:74461101-74461314 | Rare:66 | ||||
| chr15:74540966-74541273 | Common:4; Rare:108 | ||||
| chr15:74598370-74598520 | Common:1; Rare:59 | ||||
| chr15:74615559-74615898 | Common:4; Rare:107 |